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Aside from the multiple ring systems shown in the table, Naphthalene, Anthracene,Phenanthrene Chrysene,Pyrene, and Benzopyrene. Search for 1 multiple ring aromatic compound and list down its properties, sources, and uses or applications.

Aside from the multiple ring systems shown in the table, Naphthalene, Anthracene,Phenanthrene Chrysene,Pyrene, and Benzopyrene. Search for 1 multiple ring aromatic compound and list down its properties, sources, and uses or applications.

General Chemistry - Standalone book (MindTap Course List)
General Chemistry - Standalone book (MindTap Course List)
11th Edition
ISBN:9781305580343
Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
Publisher:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
Chapter11: States Of Matter; Liquids And Solids
Section: Chapter Questions
Problem 11.128QP
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Aside from the multiple ring systems shown in the table, Naphthalene, Anthracene,Phenanthrene Chrysene,Pyrene, and Benzopyrene. Search for 1 multiple ring aromatic compound and list down its properties, sources, and uses or applications.
Name and Structure Properties Uses MULTIPLE RING SYSTEMS White volatile crystals with coal tar aroma Moth repellants Fungicides Lubricants Naphthalene r.d. = 1.162 g/ml m.p. = 80.1°C b.p.= 218°C Resins Solvent Colorless, crystalline substance with violet fluorescence Source of dye Coating applications Anthracene r.d. = 1.25g/ml m.p. = 218°C b.p.= 342°C Colorless, crystalline hydrocarbon r.d. = 1.179 g/ml m.p. = 100°C b.p.= 340°C Synthesis of dyes and drugs Phenanthrene 2 | Page Polynuclear hydrocarbon which gives a bluish fluorescence Chrysene Organic synthesis r.d. = 1.274 g/ml m.p. = 254°C b.p.= 488°C Pyrene Colorless solid with blue Organic synthesis fluorescence derived from alcohol or by sublimation r.d. = 1.271 g/ml m.p. = 156°C b.p.= 404°C One of the most potent carcinogenic material found in tobacco smoke Benzopyrene Organic synthesis r.d. = 1.351g/ml m.p. = 178°C b.p.= 495°C
Transcribed Image Text:Name and Structure Properties Uses MULTIPLE RING SYSTEMS White volatile crystals with coal tar aroma Moth repellants Fungicides Lubricants Naphthalene r.d. = 1.162 g/ml m.p. = 80.1°C b.p.= 218°C Resins Solvent Colorless, crystalline substance with violet fluorescence Source of dye Coating applications Anthracene r.d. = 1.25g/ml m.p. = 218°C b.p.= 342°C Colorless, crystalline hydrocarbon r.d. = 1.179 g/ml m.p. = 100°C b.p.= 340°C Synthesis of dyes and drugs Phenanthrene 2 | Page Polynuclear hydrocarbon which gives a bluish fluorescence Chrysene Organic synthesis r.d. = 1.274 g/ml m.p. = 254°C b.p.= 488°C Pyrene Colorless solid with blue Organic synthesis fluorescence derived from alcohol or by sublimation r.d. = 1.271 g/ml m.p. = 156°C b.p.= 404°C One of the most potent carcinogenic material found in tobacco smoke Benzopyrene Organic synthesis r.d. = 1.351g/ml m.p. = 178°C b.p.= 495°C
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